KR20140048450A - Treatment agent with excellentelasticity recovery and the the knitting textile treated therewith - Google Patents

Treatment agent with excellentelasticity recovery and the the knitting textile treated therewith Download PDF

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KR20140048450A
KR20140048450A KR1020120114166A KR20120114166A KR20140048450A KR 20140048450 A KR20140048450 A KR 20140048450A KR 1020120114166 A KR1020120114166 A KR 1020120114166A KR 20120114166 A KR20120114166 A KR 20120114166A KR 20140048450 A KR20140048450 A KR 20140048450A
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mol
recovery rate
knitted fabric
elastic recovery
feeding
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KR101526931B1 (en
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조항성
이범수
허준
육지호
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한국생산기술연구원
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    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/53Polyethers
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/322Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
    • D06M13/325Amines
    • D06M13/332Di- or polyamines
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/02Natural fibres, other than mineral fibres
    • D06M2101/04Vegetal fibres
    • D06M2101/06Vegetal fibres cellulosic
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2201/00Cellulose-based fibres, e.g. vegetable fibres
    • D10B2201/01Natural vegetable fibres
    • D10B2201/02Cotton
    • DTEXTILES; PAPER
    • D10INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10BINDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
    • D10B2401/00Physical properties
    • D10B2401/06Load-responsive characteristics
    • D10B2401/061Load-responsive characteristics elastic

Abstract

The objective of the present invention is to provide a textile finishing agent having an improved elastic recovery rate and a cotton knitted fabric treated with the textile finishing agent. As the textile finishing agent having an improved elastic recovery rate, disclosed is one obtained by feeding 30 to 40 mol% of polytetramethylene ether glycol (PTMG) and 35 to 40 mol% of N-nitrosodiethanolamine (NDEA) in a reactor, raising the internal temperature to 70°C to 80°C, performing a reaction at a stirring machine rate of 200 rpm for 30 minutes, feeding 90-110 mol% of isophore diisocyanate (IPDI) and dibutyl tin dilaurate (DBTDL), lowering the temperature to 40°C if viscosity increases, feeding acetone, performing a reaction for 3 hours while maintaining the internal temperature of the reactor at 40°C if viscosity increase, feeding 35-40 mol% of 30-40% hydrochloric acid (HCl) to perform a neutralization reaction for 3 hours, feeding 18-25 mol% of ethylene diamine (EDA) to perform a chain extension reaction, feeding acetone and stirring if viscosity increases, and performing water dispersion at a stirring machine rate of 400 rpm while slowly feeding distilled water for 3 hours, after the neutralization reaction.

Description

탄성회복률이 향상된 섬유 가공제 및 이 가공제로 처리된 면섬유 편성물{Treatment agent with excellentelasticity recovery and the the knitting textile treated therewith}Textile agent with improved elastic recovery rate and cotton fiber knitted fabric treated with this agent {Treatment agent with excellentelasticity recovery and the the knitting textile treated therewith}

본 발명은 탄성회복률이 향상된 섬유 가공제 및 이 가공제로 처리된 면섬유 편성물에 관한 것으로서, 보다 상세하게는 면섬유 편성물에 적용되는 흡수성, 수축률, 탄성 및 촉감(soft touch)이 우수한 탄성회복률이 향상된 섬유 가공제 및 이 가공제로 처리된 면섬유 편성물을 제공함에 있다. The present invention relates to a fiber processing agent having an improved elastic recovery rate and a cotton fiber knitted fabric treated with the processing agent, and more particularly, a fiber processing having improved elastic recovery rate with excellent water absorption, shrinkage, elasticity and soft touch applied to the cotton fiber knitted fabric. And a cotton fiber knitted fabric treated with the processing agent.

편성물의 탄성을 증가시키기 위하여 탄성가공제로 탄성실리콘오일유화제품, 수용성 우레탄제품을 사용한다. 그러나, 상기 탄성실리콘오일유화제품은 촉감(soft touch)이 우수하지만 탄성력과 방오성이 미흡한 단점이 있다. 상기 수용성 우레탄제품은 탄성력과 흡한ㆍ속건의 특징을 가지고 있으나, 촉감(soft touch)이 미흡한 단점이 있다. In order to increase the elasticity of the knitted fabric, elastic silicone oil emulsified products and water-soluble urethane products are used as elastic processing agents. However, the elastic silicone oil emulsified product has a soft touch, but has a disadvantage of insufficient elasticity and antifouling property. The water-soluble urethane product has the characteristics of elasticity, sweat absorption and quick-drying, but has a disadvantage in that soft touch is insufficient.

상기 탄성실리콘오일유화제품 및 수용성 우레탄제품의 단점을 보완하기 위하여, 탄성실리콘오일유화제품에 수용성 우레탄이 포함되도록 가공하거나, 수용성 우레탄 합성제품에 탄성실리콘오일유화제품이 포함되도록 가공한 제품들이 있다. 그러나, 이러한 제품들 역시 저장 안정성이 나오지 않으며 촉감(soft touch)이 미흡한 것이 대부분이다. In order to supplement the shortcomings of the elastic silicone oil emulsified product and the water-soluble urethane product, there are products processed to include the water-soluble urethane in the elastic silicone oil emulsified product, or processed to include the elastic silicone oil emulsified product in the water-soluble urethane synthetic product. However, these products also lack storage stability, and most of them have a soft touch.

또한, 상기 섬유 가공제의 입자 사이즈가 500nm이상이어서, 안정성이 부족하여 끈적임(Gumming)이 발생하는 문제점이 있다. 그리하여 가공공정에서 불량률이 10%이상 나타나는 단점이 있다.In addition, since the particle size of the fiber processing agent is 500 nm or more, there is a problem that gumming occurs due to lack of stability. Thus, there is a disadvantage that the defective rate is more than 10% in the machining process.

본 발명은 면섬유 편성물에 적용되는 흡수성, 수축률, 탄성 및 촉감(soft touch)이 우수한 탄성회복률이 향상된 섬유 가공제 및 이 가공제로 처리된 면섬유 편성물을 제공함에 있다. SUMMARY OF THE INVENTION The present invention provides a fiber processing agent having an improved elastic recovery rate, which is excellent in absorbency, shrinkage, elasticity, and soft touch applied to a cotton fiber knitted fabric, and a cotton fiber knitted fabric treated with the processing agent.

또한, 본 발명은 pH 9 내지 12에서 안정성을 가지는 탄성회복률이 향상된 섬유가공제 및 이 가공제로 처리된 면섬유 편성물을 제공함에 있다.The present invention also provides a fiber processing agent having improved elastic recovery rate at a pH of 9 to 12 and a cotton fiber knitted fabric treated with the processing agent.

상기 목적을 달성하기 위해 본 발명의 일 실시예에 따른 면섬유 편성물용 섬유 가공제는 폴리테트라메틸렌 글리콜(PTMG, Polytetramethylene Ether Glycol) 30 내지 40mol% 및 니트로소디에탄올아민 (NDEA, N-nitrosodiethanolamine) 35 내지 40mol%를 반응기에 넣고 내부 온도를 70 내지 80℃로 상승한 후 교반기 속도 200rpm에서 30분 동안 반응시킨 후, 이소포론 디이소시아네이트(IPDI, isophore diisocyanate) 90 내지 110mol%와 디부틸틴디라울레이트(DBTDL, Dibutyl Tin Dilaurate) 투입하여 점도가 증가하면 온도를 40℃로 내리고 아세톤 투입한 후 점도가 낮아지면 반응기 내부 온도를 40℃로 유지하면서 3시간 동안 반응시키고, In order to achieve the above object, the fiber processing agent for cotton fiber knitted fabric according to one embodiment of the present invention is 30 to 40 mol% of polytetramethylene glycol (PTMG) and nitrosodiethanolamine (NDEA, N-nitrosodiethanolamine) 35 to After putting 40 mol% into a reactor and raising the internal temperature to 70 to 80 ° C. and reacting for 30 minutes at a stirrer speed of 200 rpm, 90 to 110 mol% of isophorone diisocyanate (IPDI) and dibutyl tin dilaurate (DBTDL, Dibutyl Tin Dilaurate) When the viscosity is increased by the addition of a viscosity, the temperature is lowered to 40 ℃ and acetone is added after the viscosity is lowered and the reaction is maintained for 3 hours while maintaining the temperature inside the reactor at 40 ℃,

염산(HCl) 30 내지 40% 35 내지 40mol%를 넣고 3시간 동안 중화반응하면서 에틸렌디아민(EDA, Ethylen diamine) 18 내지 25mol%투입하여 사슬연장 반응시키면서 점도 증가하면, 아세톤을 투입하여 교반하고, 중화반응이 끝나면 증류수를 3시간 동안 천천히 넣어주면서 교반기 속도 400rpm에서 수분산 시킨 것을 특징으로 형성될 수 있다. 30-40% hydrochloric acid (HCl) was added and 35-40 mol% was neutralized for 3 hours, and 18-25 mol% of ethylenediamine (EDA, Ethylen diamine) was added thereto. After the reaction can be formed, characterized in that the distilled water was slowly added for 3 hours while being dispersed in the stirrer speed 400rpm.

상기 탄성회복률이 향상된 섬유 가공제는 실리콘과 1:1로 합성된 농도가 9 내지 12pH 인 것을 특징으로 형성될 수 있다.The fiber recovery agent with improved elastic recovery rate may be formed of a concentration of 9 to 12pH synthesized 1: 1 with silicon.

상기 탄성회복률이 향상된 섬유 가공제는 냉각 후 입자의 사이즈가 40nm 내지 50nm 인 것을 특징으로 형성될 수 있다.The fiber processing agent having improved elastic recovery rate may be formed after the cooling has a particle size of 40nm to 50nm.

또한, 본 발명의 면섬유 편성물은 폴리테트라메틸렌 글리콜(PTMG, Polytetramethylene Ether Glycol) 30 내지 40mol% 및 니트로소디에탄올아민 (NDEA, N-nitrosodiethanolamine) 35 내지 40mol%를 반응기에 넣고 내부 온도를 70 내지 80℃로 상승한 후 교반기 속도 200rpm에서 30분 동안 반응시킨 후, 이소포론 디이소시아네이트(IPDI, isophore diisocyanate) 90 내지 110mol%와 디부틸틴디라울레이트(DBTDL, Dibutyl Tin Dilaurate) 투입하여 점도가 증가하면 온도를 40℃로 내리고 아세톤 투입한 후 점도가 낮아지면 반응기 내부 온도를 40℃로 유지하면서 3시간 동안 반응시키고, 염산(HCl) 30 내지 40% 35 내지 40mol%를 넣고 3시간 동안 중화반응하면서 에틸렌디아민(EDA, Ethylen diamine) 18 내지 25mol%투입하여 사슬연장 반응시키면서 점도 증가하면, 아세톤을 투입하여 교반하고, 중화반응이 끝나면 증류수를 3시간 동안 천천히 넣어주면서 교반기 속도 400rpm에서 수분산 시킨 탄성회복률이 향상된 섬유 가공제로 면섬유 편성물이 가공처리 된 것을 특징으로 형성될 수 있다.In addition, the cotton fiber knitted fabric of the present invention is 30 to 40 mol% polytetramethylene glycol (PTMG, Polytetramethylene Ether Glycol) and 35 to 40 mol% nitrosodieethanolamine (NDEA) in the reactor and the internal temperature is 70 to 80 ℃ After the reaction was carried out for 30 minutes at a stirrer speed of 200 rpm, 90 to 110 mol% of isophorone diisocyanate (IPDI) and dibutyl tin dilaurate (DBTDL) were added to increase the viscosity. After lowering to ℃ and adding acetone, the viscosity was lowered and reacted for 3 hours while maintaining the temperature inside the reactor at 40 ℃, and 30 to 40% hydrochloric acid (HCl) was added to 35 to 40mol% and neutralized for 3 hours while ethylenediamine (EDA , Ethylen diamine) Add 18 to 25 mol% of chain lengthening reaction while increasing the viscosity, add acetone and stir, and after neutralization reaction distilled water for 3 hours Not while slowly put agitator speed was 400rpm elastic recovery The fiber processing agent improved cotton fiber knitted be distributed in this form may be characterized in that the processing operation.

상기 면섬유 편성물은 탄성회복률이 90 내지 95%인 것을 특징으로 형성될 수 있다. The cotton fiber knitted fabric may be formed, characterized in that the elastic recovery rate is 90 to 95%.

상기 면섬유 편성물은 수축률이 0 내지 3%인 것을 특징으로 형성될 수 있다. The cotton fiber knitted fabric may be formed, characterized in that the shrinkage is 0 to 3%.

상기와 같이 하여, 본 발명에 의한 면섬유 편성물용 섬유 가공제 및 이 섬유 가공제로 처리된 면섬유 편성물은 포름알데히드가 검출되지 않는 친환경 섬유가공제를 제공할 수 있다. As described above, the fiber processing agent for the cotton fiber knitted fabric according to the present invention and the cotton fiber knitted fabric treated with the fiber processing agent can provide an eco-friendly fiber processing agent in which formaldehyde is not detected.

또한, 본 발명에 의한 면섬유 편성물용 섬유 가공제는 pH 9 내지 12에서 안정성을 가지기 때문에 실리콘오일의 깨짐 현상 및 끈적임(Gumming)이 제거되어 면섬유 편성물의 가공공정에서 불량률이 저하되는 효과가 있다.In addition, since the fiber processing agent for cotton fiber knitted fabric according to the present invention has a stability at pH 9 to 12, the cracking phenomenon and the sticking (gumming) of the silicone oil are removed, thereby reducing the defect rate in the processing process of the cotton fiber knitted fabric.

또한, 본 발명은 수분산 우레탄에 실리콘오일을 합성한 면섬유 편성물용 섬유 가공제를 제공하며, 이 섬유 가공제로 처리된 면섬유 편성물에는 탄성회복률, 수축률, 황변, 탄성 및 촉감(soft touch)이 우수한 효과가 있다. In addition, the present invention provides a fiber processing agent for cotton fiber knitted fabrics in which silicone oil is synthesized in a water-dispersed urethane, and the cotton fiber knitted fabric treated with this fiber processing agent has excellent elastic recovery rate, shrinkage ratio, yellowing, elasticity and soft touch. There is.

도 1은 본 발명의 일 실시예에 따른 탄성회복률이 향상된 섬유 가공제의 합성공정을 개략적으로 도시한 공정도이다.
도 2는 본 발명의 일 실시예에 따른 탄성회복률이 향상된 섬유 가공제의 화학 구조식을 도시한 것이다.
도 3은 본 발명의 일 실시예에 따른 탄성회복률이 향상된 섬유 가공제의 pH 안정도를 실험한 샘플의 사진이다.
1 is a process diagram schematically showing the synthesis process of the fiber processing agent is improved elastic recovery rate according to an embodiment of the present invention.
Figure 2 shows the chemical structural formula of the fiber processing agent is improved elastic recovery rate according to an embodiment of the present invention.
Figure 3 is a photograph of a sample experiments to test the pH stability of the improved fiber recovery agent according to an embodiment of the present invention.

본 발명이 속하는 기술분야에 있어서 통상의 지식을 가진 자가 용이하게 실시할 수 있을 정도로 본 발명의 바람직한 실시예를 상세하게 설명하면 다음과 같다.
Hereinafter, exemplary embodiments of the present invention will be described in detail so that those skilled in the art can easily practice the present invention.

이하에서는 본 발명에 일 실시예에 따른 탄성회복률이 향상된 섬유 가공제를 설명하도록 한다. Hereinafter, to describe the fiber processing agent improved the elastic recovery rate according to an embodiment of the present invention.

상기 탄성회복률이 향상된 섬유 가공제는, 도 1 내지 도 2를 참조하면, 폴리테트라메틸렌 글리콜(PTMG, Polytetramethylene Ether Glycol) 30 내지 40mol% 및 니트로소디에탄올아민 (NDEA, N-nitrosodiethanolamine) 35 내지 40mol%를 반응기에 넣고 내부 온도를 70 내지 80℃로 상승한 후 교반기 속도 200rpm에서 30분 동안 반응시킨 후, 이소포론 디이소시아네이트(IPDI, isophore diisocyanate) 90 내지 110mol%와 디부틸틴디라울레이트(DBTDL, Dibutyl Tin Dilaurate) 투입하여 점도가 증가하면 온도를 40℃로 내리고 아세톤 투입한 후 점도가 낮아지면 반응기 내부 온도를 40℃로 유지하면서 3시간 동안 반응시키고, 염산(HCl) 30 내지 40% 35 내지 40mol%를 넣고 3시간 동안 중화반응하면서 에틸렌디아민(EDA, Ethylen diamine) 18 내지 25mol%투입하여 사슬연장 반응시키면서 점도 증가하면, 아세톤을 투입하여 교반하고, 중화반응이 끝나면 증류수를 3시간 동안 천천히 넣어주면서 교반기 속도 400rpm에서 수분산 시킨 것이다. The fiber recovery agent with improved elastic recovery rate, referring to Figures 1 to 2, polytetramethylene glycol (PTMG, Polytetramethylene Ether Glycol) 30 to 40 mol% and nitrosodiethanolamine (NDEA, N-nitrosodiethanolamine) 35 to 40 mol% After the reaction was carried out for 30 minutes at a stirrer speed of 200 rpm, the internal temperature was raised to 70 to 80 ° C., and then 90 to 110 mol% of isophorone diisocyanate (IPDI) and dibutyl tin dilaurate (DBTDL, Dibutyl Tin) were added. Dilaurate) When the viscosity is increased by adding the acetone, the temperature is lowered to 40 ° C, and when the acetone is added, the viscosity is lowered and the reaction is continued for 3 hours while maintaining the temperature inside the reactor at 40 ° C, and hydrochloric acid (HCl) 30-40% 35-40mol% Put neutralization reaction for 3 hours, add 18-25 mol% of ethylenediamine (EDA, Ethylen diamine), increase the viscosity while chain-reacting, add acetone and stir, After the neutralization reaction, distilled water was added slowly for 3 hours and dispersed at 400rpm.

상기 탄성회복률이 향상된 섬유 가공제는, 도3을 참조하면, H 9 내지 12에서 안정성을 가지는 것을 확인 할 수 있었다.
The fiber processing agent improved the elastic recovery rate, it can be seen that having a stability in H 9 to 12, referring to FIG.

이하, 본 발명을 하기의 실시예 및 비교예에 의거하여 좀 더 상세하게 설명한다. 단, 하기 실시예는 본 발명을 예시하기 위한 것일 뿐, 본 발명이 하기 실시예에 의하여 한정되는 것이 아니고, 본 발명의 기술적 사상을 벗어나지 않는 범위 내에서 치환 및 균등한 타 실시예로 변경할 수 있음은 본 발명이 속하는 기술분야에서 통상의 지식을 가진 자에게 있어서 명백할 것이다.
Hereinafter, the present invention will be described in more detail based on the following Examples and Comparative Examples. However, the following examples are only for illustrating the present invention, and the present invention is not limited to the following examples and may be changed to other embodiments equivalent to substitutions and equivalents without departing from the technical spirit of the present invention. Will be apparent to those of ordinary skill in the art.

제1 실시예First Embodiment

폴리테트라메틸렌 글리콜(PTMG, Polytetramethylene Ether Glycol) 40mol%와 니트로소디에탄올아민 (NDEA, N-nitrosodiethanolamine) 38mol%를 반응기에 넣고 내부 온도를 75℃로 상승한 후 교반기 속도 200rpm에서 30분 동안 반응시킨 후, 이소포론 디이소시아네이트(IPDI, isophore diisocyanate) 100mol%와 디부틸틴디라울레이트(DBTDL, Dibutyl Tin Dilaurate) 투입, 점도가 증가하면 온도를 40℃로 내리고 아세톤 투입하고, 점도가 낮아지면 3시간 동안 반응시킨다. 이 때, 반응기 내부 온도를 40℃로 유지, 염산(HCl) 35% 38mol%를 넣고 3시간 동안 중화반응하면서 에틸렌디아민(EDA, Ethylen diamine) 19mol%투입하여 사슬연장 반응시킨다. 점도 증가하면, 아세톤 투입 후 교반하고, 중화반응이 끝나면 증류수를 3시간 동안 천천히 넣어주면서 교반기 속도 400rpm에서 수분산 시킨 일액형 섬유 가공제를 제조한다.40 mol% of polytetramethylene glycol (PTMG) and 38 mol% of nitrosodiethanolamine (NDEA) were added to the reactor, and the internal temperature was raised to 75 ° C., followed by reaction at a stirrer speed of 200 rpm for 30 minutes. 100 mol% of isophorone diisocyanate (IPDI) and dibutyl tin dilaurate (DBTDL) are added.If the viscosity is increased, the temperature is lowered to 40 ° C and acetone is added. . At this time, the reactor inside temperature is maintained at 40 ℃, hydrochloric acid (HCl) 35% 38mol% and neutralization reaction for 3 hours while ethylenediamine (EDA, Ethylen diamine) is added to the chain extension reaction. When the viscosity is increased, acetone is added and stirred, and when the neutralization reaction is finished, distilled water is slowly added for 3 hours to prepare a one-component fiber processing agent that is dispersed at a stirrer speed of 400 rpm.

상기 제조된 가공제는 고형분 24.34%, 입자사이즈가 42.9nm으로 형성된다.
The prepared processing agent has a solid content of 24.34% and a particle size of 42.9 nm.

상기 실시예 1은 제조된 가공제의 성능을 테스트하기 위하여 30cm×30cm 40's 면니트를 Pad(1bar) → Dry(120℃×2min) → Cure(170℃×2min)의 방법으로 처리한 후 가공처리된 원단의 수축율을 실험하였다. 상기 실시예1의 pH 농도는 10%인 것을 특징으로 한다. In Example 1, 30cm × 30cm 40's cotton knit was treated by Pad (1bar) → Drying (120 ℃ × 2min) → Cure (170 ℃ × 2min) to test the performance of the manufactured processing agent. The shrinkage of the fabric was examined. The pH concentration of Example 1 is characterized in that 10%.

비교예1은 실리콘(pH 8%)과 보조제(pH 6%)가 혼합된 이액형 섬유 가공제로 가공처리된 것이다. Comparative Example 1 was processed with a two-component fiber processing agent in which silicon (pH 8%) and an auxiliary agent (pH 6%) were mixed.

비교예2는 실리콘(pH 6%), 일반유연제(pH 4%) 및 혼합 가공제(pH 10%)가 혼합된 삼액형 섬유 가공로 가공처리된 것이다.
Comparative Example 2 was processed by three-component fiber processing in which silicon (pH 6%), general softener (pH 4%) and mixed processing agent (pH 10%) were mixed.

표1은 실시예1, 비교예1 및 비교예2의 섬유가공제의 농도별 수축율의 변화를 실험한 것이다. Table 1 is a test of the change in the shrinkage rate of each of the fiber processing agent of Example 1, Comparative Example 1 and Comparative Example 2.

Figure pat00001
Figure pat00001

실시예1은 수축률이 0%로 이액형 가공제인 비교예1과 삼액형 가공제인 비교예2로 가공된 원단보다 수축률이 우수한 것임을 확인하였다. In Example 1, the shrinkage was 0%, and it was confirmed that the shrinkage was superior to the fabric processed in Comparative Example 1, which is a two-component processing agent, and Comparative Example 2, which was a three-component processing agent.

표2는 실시예1의 제조방법과 동일한 방법으로 섬유 가공제를 제조한 후 pH의 농도를 변화시킨 다음 ph 농도 별 수축률을 실험한 것이다. Table 2 shows the shrinkage rate for each ph concentration after the fabrication of the fiber processing agent in the same manner as in Example 1 after changing the concentration of pH.

Figure pat00002
Figure pat00002

실시예2는 비교예2의 수축률보다 향상된 결과를 얻을 수 있었으며, pH 농도가 10%인 경우에 수축률이 0%가 되어 최적의 효과를 가지고, 15 내지 20%에서 수축율이 증가하지만 비교예의 삼액형 가공제보다 우수한 효과를 가지는 것을 확인하였다. Example 2 was able to obtain an improved result than the shrinkage of Comparative Example 2, when the pH concentration is 10% has an optimum effect of the shrinkage is 0%, the shrinkage is increased from 15 to 20%, but the three-component type of Comparative Example It confirmed that it had an effect superior to a processing agent.

따라서, 수축율에 있어서, 농도가 5 내지 15%인 것을 특징으로 형성될 수 있으나, 바람직하게는 가공제의 농도가 10%인 것을 특징으로 한다. 가공제의 농도가 10%일 때, 수축율이 0로 가장 우수한 효과를 나타내었다.
Therefore, in the shrinkage rate, the concentration may be formed from 5 to 15%, preferably, the concentration of the processing agent is characterized in that 10%. When the concentration of the processing agent was 10%, the shrinkage ratio was 0, showing the best effect.

표3은 가공원단을 5cm ? 15cm로 자른 후 두 클램프 사이의 거리를 10cm로 한 후 양 끝을 물린 후 사이 거리를 표시 한 후 17cm(170%)로 늘린 후 10분간 고정, 물린 클램프를 풀고 1시간 동안 수축된 길이 측정한 것이다. 하기 표3에서 참고예는 가공처리 되지 않은 원단의 탄성 회복률을 측정한 것이다.Table 3 shows 5cm? After cutting to 15cm, the distance between the two clamps is 10cm, and the distance between the two clamps is indicated, and the distance between the two clamps is displayed.Then, the distance is increased to 17cm (170%), and fixed for 10 minutes. . In the following Table 3 is a reference to measure the elastic recovery of the untreated fabric.

Figure pat00003
Figure pat00003

탄성 회복률에 있어서, 농도가 5 내지 15%인 것을 특징으로 하며, 바람직하게는 가공제의 농도가 10%인 것을 특징으로 한다. 가공제 농도는 10%일 때, 탄성 회복률이 92.86으로 가장 우수한 효과를 나타내었다.
In the elastic recovery rate, the concentration is characterized in that 5 to 15%, preferably the concentration of the processing agent is characterized in that 10%. When the concentration of the processing agent was 10%, the elastic recovery rate was 92.86, showing the best effect.

표4는 실시예1를 기준으로 실리콘(si) 함량을 변화시켜 색상의 변화를 실험한 것이다. Table 4 shows the experiment of the color change by changing the silicon (si) content based on Example 1.

Figure pat00004
Figure pat00004

황변에 있어서, 실리콘(si) 농도가 증가할수록 백도(whiteness)값이 증가하는 것을 알 수 있다.
In yellowing, it can be seen that as the concentration of silicon (si) increases, the whiteness value increases.

이상 설명한 바와 같이, 본 발명은 상술한 특정의 바람직한 실시예에 한정되지 아니하며, 특허청구범위에서 청구하는 본 발명의 요지를 벗어남이 없이 당해 발명이 속하는 기술분야에서 통상의 지식을 가진 자라면 누구든지 다양한 변형의 실시가 가능한 것은 물론이고, 그와 같은 변경은 특허청구범위 기재의 범위 내에 있게 된다.
As described above, the present invention is not limited to the specific preferred embodiments described above, and any person having ordinary skill in the art to which the present invention pertains without departing from the gist of the present invention claimed in the claims. Various modifications are possible, of course, and such changes are within the scope of the claims.

Claims (6)

폴리테트라메틸렌 글리콜(PTMG, Polytetramethylene Ether Glycol) 30 내지 40mol% 및 니트로소디에탄올아민 (NDEA, N-nitrosodiethanolamine) 35 내지 40mol%를 반응기에 넣고 내부 온도를 70 내지 80℃로 상승한 후 교반기 속도 200rpm에서 30분 동안 반응시킨 후, 이소포론 디이소시아네이트(IPDI, isophore diisocyanate) 90 내지 110mol%와 디부틸틴디라울레이트(DBTDL, Dibutyl Tin Dilaurate) 투입하여 점도가 증가하면 온도를 40℃로 내리고 아세톤 투입한 후 점도가 낮아지면 반응기 내부 온도를 40℃로 유지하면서 3시간 동안 반응시키고,
염산(HCl) 30 내지 40% 35 내지 40mol%를 넣고 3시간 동안 중화반응하면서 에틸렌디아민(EDA, Ethylen diamine) 18 내지 25mol%투입하여 사슬연장 반응시키면서 점도 증가하면, 아세톤을 투입하여 교반하고, 중화반응이 끝나면 증류수를 3시간 동안 천천히 넣어주면서 교반기 속도 400rpm에서 수분산 시킨 것을 특징으로 하는 탄성회복률이 향상된 섬유 가공제.
30-40 mol% of polytetramethylene glycol (PTMG) and 35-40 mol% of nitrosodiethanolamine (NDEA) were added to the reactor, and the internal temperature was raised to 70-80 ° C. After reacting for a minute, 90-110 mol% of isophorone diisocyanate (IPDI) and dibutyl tin dilaurate (DBTDL) were added to increase the viscosity, and then the temperature was lowered to 40 ° C. and acetone was added. When lowered to react for 3 hours while maintaining the temperature inside the reactor at 40 ℃,
30-40% hydrochloric acid (HCl) was added and 35-40 mol% was neutralized for 3 hours, and 18-25 mol% of ethylenediamine (EDA, Ethylen diamine) was added thereto. When the reaction is completed, the fiber recovery agent with improved elastic recovery rate, characterized in that the distilled water was slowly added for 3 hours and dispersed at a stirrer speed of 400rpm.
제 1 항에 있어서,
상기 탄성회복률이 향상된 섬유 가공제는 실리콘과 1:1로 합성된 농도가 9 내지 12pH 인 것을 특징으로 하는 탄성회복률이 향상된 섬유 가공제.
The method according to claim 1,
The fiber recovery agent with improved elastic recovery rate is an elastic recovery rate improved fiber processing agent, characterized in that the concentration of 1 to 12pH synthesized with silicon 1: 1.
제 1 항에 있어서,
상기 탄성회복률이 향상된 섬유 가공제는 냉각 후 입자의 사이즈가 40nm 내지 50nm 인 것을 특징으로 하는 탄성회복률이 향상된 섬유 가공제.
The method according to claim 1,
The fiber recovery agent having improved elastic recovery rate, the fiber recovery agent with improved elastic recovery rate, characterized in that the particle size of 40nm to 50nm after cooling.
제 1 항 또는 제 3 항 중 어느 한 항의 탄성회복률이 향상된 섬유 가공제로 면섬유 편성물이 가공처리 된 것을 특징으로 하는 면섬유 편성물.The cotton fiber knitted fabric of claim 1 or 3, wherein the cotton fiber knitted fabric is processed with the fiber processing agent having improved elastic recovery rate. 제 4 항에 있어서,
상기 면섬유 편성물은 탄성회복률이 90 내지 95%인 것을 특징으로 하는 면섬유 편성물.
5. The method of claim 4,
The cotton fiber knitted fabric is a cotton fiber knitted fabric, characterized in that the recovery rate of 90 to 95%.
제 4 항에 있어서,
상기 면섬유 편성물은 수축률이 0 내지 3%인 것을 특징으로 하는 면섬유 편성물.
5. The method of claim 4,
The cotton fiber knitted fabric is a cotton fiber knitted fabric, characterized in that the shrinkage of 0 to 3%.
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